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Assistant Manager Manufacturing Quality


Visakhapatnam, AP 530003
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Job Details

The Manufacturing Quality Supervisor is responsible for ensuring Sterilization, Visual Inspection, and Packaging are operating under a state of cGMP compliance. The Supervisor is directly responsible for managing and coordinating all quality functions within the area. The individual must communicate effectively and work with cross-functional teams.


+ Supervise a specific shift to ensure that Terminal Sterilization, Visual Inspection & Packaging areas are operating within a state of cGMP compliance

+ Facilitate achievement and maintenance of quality goals and cGMP compliance

+ Collaborate with manufacturing management to identify and correct product and/or process defects

+ Accountable for ensuring products meet cGMP requirements

+ Ensure that when quality related issues arise, these issues are quickly escalated, so that documentation of events, investigations, and corrective actions are performed in a timely manner

+ Manage deviations and prevent future occurrences by identifying root causes, enhance the capture of data for investigations, and implement effective CAPAs

+ Manage quality project initiatives

+ Maintain regulatory compliance by building and sustaining quality concepts

+ Conduct audits / walkthroughs to ensure procedures are being followed in accordance with cGMP

+ Provides guidance and mentorship to direct reports on quality concepts


B. Pharm/M. Pharma/M. Sc. plus a minimum of 5 years working in sterile dosage manufacturing facility

+ Leadership and decision making abilities

+ Strong interpersonal skills

+ Analytical mind to grasp complex analytical issues and provide feasible, logical and scientific solutions

+ Communication skills to provide feedback and mentoring to QA colleagues and internal customers

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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